This study aims to verify the concept of niches at multiple spatial scales in plant communities.To this end,we analyzed the niche characteristic of Rhododendron dauricum plant communities in Northeast China at three s...This study aims to verify the concept of niches at multiple spatial scales in plant communities.To this end,we analyzed the niche characteristic of Rhododendron dauricum plant communities in Northeast China at three spatial scales.At the local scale,we calculated the Importance Value(IV)of species in five communities in the north of the Da Hinggan Mountains.At the intermediate scale,we examined five communities in their entirety,calculated the niche breadth of the species,and integrated niche overlap and interspecific association to analyze interspecific relationships.Further,the generalized additive model(GAM)was used to analyze the impact of topography and soil factors on niche characteristics.At the regional scale,we analyzed the geographical distribution of dominant species of R.dauricum plant communities in Northeast China and used principal component analysis(PCA)to analyze the impact of geographical and climate factors on species distribution.The results show that at the local scale,the IV of the species in each community varies widely.At the intermediate scale,species with a wide niche breadth tend to have a high value for IV.Larix gmelinii,Betula platyphylla,R.dauricum,Ledum palustre,and Vaccinium vitis-idaea had a relatively wide niche breadth and a high niche overlap,and the interspecific associations were almost all positive.Elevation and soil nutrients were the most dominant environmental factors.At the regional scale,species with a wide niche breadth tend to have a wide range of distribution,and temperature and precipitation were the most dominant environmental factors.This study suggests that the niche characteristics at three scales are both related and different.Niche characteristics at the local scale were various and labile,and niche characteristics at the intermediate and regional scales were relatively regular.These results show some degree of consistency with previous studies from an evolutionary perspective.The action mechanisms of these communities are related to differences in the dominant environmental factors.In addition,the integration of niche overlap and interspecific association determine interspecific relationships more accurately.展开更多
[Objective] The aim of this study was to further investigate and utilize the natural anthocyanidin from Rhododendron L. [Method] Using Rhododendron L. with four different colors including white, pink, red and purple a...[Objective] The aim of this study was to further investigate and utilize the natural anthocyanidin from Rhododendron L. [Method] Using Rhododendron L. with four different colors including white, pink, red and purple as the test materials, its anthocyanidin extraction methods were analyzed in this study to evaluate the spectral properties and its stability of various anthocyanidin. [Result] The anthocyanidin from Rhododendron L. was perfectly extracted by methanol with 1% concentrated hydrochloric acid (V/V) and had better stability in this extraction solution. The further experiment in vitro indicated that the anthocyanidin from Rhododendron L. became stable with pH value of 0-3, but could not resistant to high temperature or strong light, and the alkaline condition had also great effects on its stability. [Conclusion] The methanol with 1% concentrated hydrochloric acid (V/V) has the best effect for extraction, and the anthocyanidin from Rhododendron L. is more stable in low temperature, weak light and acid conditions.展开更多
The extract from leaves of Rhododendron dauricum L. was extracted with 95% alcohol by common method for studying its insecticidal activities. The chemical components of the alcohol extract and relative contents were a...The extract from leaves of Rhododendron dauricum L. was extracted with 95% alcohol by common method for studying its insecticidal activities. The chemical components of the alcohol extract and relative contents were analyzed by GC-MS. The insecticidal activities of the alcohol extract were tested on the 2nd？3rd instar larvae of Lymantria dispar L. for five days. Five concentrations of the extract samples were designed as 50, 10, 5, 1, and 0.5 g？L？1. The results show that the alcohol extracts from leaves of R. dauricum exhibited insecticidal activities against larvae of L. dispar. The corrected mortality of larvae of L. dispar for was over 50% for both contact toxicity and stomach toxicity at the extract concentration of ≥ 5 g·L？1 after five days of application. The insecticidal activity in contact toxicity is more effect than stomach toxicity for the alcohol extract. Twenty compounds, with total GC relative contents of 93.81% in the alcohol extract from leaves of R. dauricum were identified. The main chemical components in the extract are： （1） 4,5-Dihydro-5-oxo-3-（p-tolyl） isoxazole, with a relative content of 40.03%; （2） 1,3-Benzenediol, 5-methyl-2-（3,7,11-trimethyl-2,6,10- dodecatrienyl）-, （E,E）-, the relative content 18.27%; （3） 3,6-Diphenyl- 1,2,3,4,5,6,7,8-octahydro-1,8-acridinedione, the relative content 3.89%; （4） 6H-[1,2,4]Triazolo[1,5-a]indole, 4a,5,7,8,8a,9-hexahydro-9- methylene-, the relative content 2.99%; （5） 7-Amino-4-methyl-1,8- naphthyridin-2-ol, the relative content 2.64%; （6） 4-Methyl-2,6- dihydroxyquinoline, the relative content 2.63%; （7） 2,4,6- Triaminoquinazoline, the relative content 2.27%; （8） 2（1H）-Quinolinone, 4-hydroxy-1-methyl-, the relative content 2.02%.展开更多
A novel diterpenoid with an unprecedented 5/6/5/7 tetracyclic system, rhodauricanol A(1), five new grayanane-derived diterpenoids, dauricanols A-E(2-6), and five known ones(7-11) were isolated from the flowers of Rhod...A novel diterpenoid with an unprecedented 5/6/5/7 tetracyclic system, rhodauricanol A(1), five new grayanane-derived diterpenoids, dauricanols A-E(2-6), and five known ones(7-11) were isolated from the flowers of Rhododendron dauricum. Rhodauricanol A(1) possesses a unique 5/6/5/7 tetracyclic ring system featuring a 16-oxa-tetracyclo[11.2.1.0^(1,5).0^(7,13)]hexadecane core. Dauricanols A-C(2-4) are the first1,3-dioxolane conjugates of grayanane diterpenoids and 5-hydroxymethylfurfural and vanillin, respectively, and dauricanols D(5) and E(6) represent the first examples of 6-deoxy-1,5-seco-grayanane diterpenoids. Their structures were determined by spectroscopic methods, quantum chemical calculation including ^(13)C NMR-DP4+ analysis and ECD calculation, and single-crystal X-ray diffraction analysis. Plausible biosynthetic pathways for 1-4 were proposed. All the isolates showed significant analgesic activities,and dauricanols B(3) and C(4) showed more potent analgesic activities than the positive control, morphine.展开更多
Kalmane diterpenoids,featuring a 5/8/5/5 tetracyclic carbon skeleton,are very rare in nature.The flowers of Rhododendron dauricum L.(Ericaceae)were phytochemically investigated for the first time,leading to the isolat...Kalmane diterpenoids,featuring a 5/8/5/5 tetracyclic carbon skeleton,are very rare in nature.The flowers of Rhododendron dauricum L.(Ericaceae)were phytochemically investigated for the first time,leading to the isolation of eight kalmane diterpenoids(1-8)including four new ones,named rhodokalmanols A-D(1-4).The structures of 1-8 were elucidated by comprehensive spectroscopic methods and ic NMR-DP4+analysis,and the absolute configurations of 1,2,4,and 5 were defined by single-crystal X-ray diffraction analysis with Cu Kαradiation.Rhodokalmanol A(1)represents the first 5,8-epoxykalmane diterpenoid and also the first kalm-15(16)-ene diterpenoid.Rhodokalmanols BD(2-4)are the first examples of kalm-7(8)-ene,kalm-16(17)-ene,and 8α-methoxykalmane diterpenoids,respectively.All the isolated kalmane diterpenoids 1-8 exhibited significant analgesic effects,and rhodokalmanol C(3)and kalmanoi(8)expressed more potent analgesic activity than morphine at doses of 0.2 and 0.04 mg/kg.The preliminary structure-activity relationships of kalmane diterpenoids as potent analgesics are discussed.展开更多
The present study was designed to determine the major chemical constituents of the leaves of Rhododendron dauricum L. Compounds were isolated and purified by various chromatographic methods, and their structures were ...The present study was designed to determine the major chemical constituents of the leaves of Rhododendron dauricum L. Compounds were isolated and purified by various chromatographic methods, and their structures were elucidated by physicochemical properties and spectral data. The present study identified two new C-methyl flavanones, 5, 7, 3', 5'-tetrahydroxy-6, 8-di-C-methyl flavanone(1) and 5, 4'-dihydroxy-8-C-methylflavanone-7-O-β-D-glucopyranoside(2), and one new flavonoid glycoside, quercetin-3-O-β-D-(6''-O-cinnamoyl)-galactoside(3), along with seven known compounds, including syzalterin(4), poriolin(5), farrerol-7-O-β-D-glucopyranoside(6), myrciacetin(7), quercetin-3-O-β-D-(6-p-hydroxy-benzoyl)-galactoside(8), quercetin-3-O-β-D-(6-p-coumaroyl)-galactoside(9), and 5, 7, 3', 5'-tetrahydroxyl flavanone(10). Compounds 1-3 were determined to be new flavonoids; compounds 4-6 were isolated from this species for the first time; and compounds 7-10 were reported for the first time from this genus.展开更多
基金Under the auspices of National Key Research and Development Program of China(No.2016YFC0500306)。
文摘This study aims to verify the concept of niches at multiple spatial scales in plant communities.To this end,we analyzed the niche characteristic of Rhododendron dauricum plant communities in Northeast China at three spatial scales.At the local scale,we calculated the Importance Value(IV)of species in five communities in the north of the Da Hinggan Mountains.At the intermediate scale,we examined five communities in their entirety,calculated the niche breadth of the species,and integrated niche overlap and interspecific association to analyze interspecific relationships.Further,the generalized additive model(GAM)was used to analyze the impact of topography and soil factors on niche characteristics.At the regional scale,we analyzed the geographical distribution of dominant species of R.dauricum plant communities in Northeast China and used principal component analysis(PCA)to analyze the impact of geographical and climate factors on species distribution.The results show that at the local scale,the IV of the species in each community varies widely.At the intermediate scale,species with a wide niche breadth tend to have a high value for IV.Larix gmelinii,Betula platyphylla,R.dauricum,Ledum palustre,and Vaccinium vitis-idaea had a relatively wide niche breadth and a high niche overlap,and the interspecific associations were almost all positive.Elevation and soil nutrients were the most dominant environmental factors.At the regional scale,species with a wide niche breadth tend to have a wide range of distribution,and temperature and precipitation were the most dominant environmental factors.This study suggests that the niche characteristics at three scales are both related and different.Niche characteristics at the local scale were various and labile,and niche characteristics at the intermediate and regional scales were relatively regular.These results show some degree of consistency with previous studies from an evolutionary perspective.The action mechanisms of these communities are related to differences in the dominant environmental factors.In addition,the integration of niche overlap and interspecific association determine interspecific relationships more accurately.
基金Supported by Natural Science Foundation (30860120 )Scientific Planning Project of Jiangxi Provincial Education Department(GJJ08159)+1 种基金Initiating Fund for Doctors in Jiangxi Normal University(1881)Development Fund for youth in Jiangxi Normal University(2398)~~
文摘[Objective] The aim of this study was to further investigate and utilize the natural anthocyanidin from Rhododendron L. [Method] Using Rhododendron L. with four different colors including white, pink, red and purple as the test materials, its anthocyanidin extraction methods were analyzed in this study to evaluate the spectral properties and its stability of various anthocyanidin. [Result] The anthocyanidin from Rhododendron L. was perfectly extracted by methanol with 1% concentrated hydrochloric acid (V/V) and had better stability in this extraction solution. The further experiment in vitro indicated that the anthocyanidin from Rhododendron L. became stable with pH value of 0-3, but could not resistant to high temperature or strong light, and the alkaline condition had also great effects on its stability. [Conclusion] The methanol with 1% concentrated hydrochloric acid (V/V) has the best effect for extraction, and the anthocyanidin from Rhododendron L. is more stable in low temperature, weak light and acid conditions.
文摘The extract from leaves of Rhododendron dauricum L. was extracted with 95% alcohol by common method for studying its insecticidal activities. The chemical components of the alcohol extract and relative contents were analyzed by GC-MS. The insecticidal activities of the alcohol extract were tested on the 2nd？3rd instar larvae of Lymantria dispar L. for five days. Five concentrations of the extract samples were designed as 50, 10, 5, 1, and 0.5 g？L？1. The results show that the alcohol extracts from leaves of R. dauricum exhibited insecticidal activities against larvae of L. dispar. The corrected mortality of larvae of L. dispar for was over 50% for both contact toxicity and stomach toxicity at the extract concentration of ≥ 5 g·L？1 after five days of application. The insecticidal activity in contact toxicity is more effect than stomach toxicity for the alcohol extract. Twenty compounds, with total GC relative contents of 93.81% in the alcohol extract from leaves of R. dauricum were identified. The main chemical components in the extract are： （1） 4,5-Dihydro-5-oxo-3-（p-tolyl） isoxazole, with a relative content of 40.03%; （2） 1,3-Benzenediol, 5-methyl-2-（3,7,11-trimethyl-2,6,10- dodecatrienyl）-, （E,E）-, the relative content 18.27%; （3） 3,6-Diphenyl- 1,2,3,4,5,6,7,8-octahydro-1,8-acridinedione, the relative content 3.89%; （4） 6H-[1,2,4]Triazolo[1,5-a]indole, 4a,5,7,8,8a,9-hexahydro-9- methylene-, the relative content 2.99%; （5） 7-Amino-4-methyl-1,8- naphthyridin-2-ol, the relative content 2.64%; （6） 4-Methyl-2,6- dihydroxyquinoline, the relative content 2.63%; （7） 2,4,6- Triaminoquinazoline, the relative content 2.27%; （8） 2（1H）-Quinolinone, 4-hydroxy-1-methyl-, the relative content 2.02%.
基金supported by the Fund of State Key Laboratory of Phytochemistry and Plant Resources in West China (NoP2022-KF08)National Natural Science Foundation of China (Nos.22107033 and U1703109)the Scientific Research Project of Traditional Chinese Medicine of Hubei Provincial Health Commission (No. ZY2021M056)。
文摘A novel diterpenoid with an unprecedented 5/6/5/7 tetracyclic system, rhodauricanol A(1), five new grayanane-derived diterpenoids, dauricanols A-E(2-6), and five known ones(7-11) were isolated from the flowers of Rhododendron dauricum. Rhodauricanol A(1) possesses a unique 5/6/5/7 tetracyclic ring system featuring a 16-oxa-tetracyclo[11.2.1.0^(1,5).0^(7,13)]hexadecane core. Dauricanols A-C(2-4) are the first1,3-dioxolane conjugates of grayanane diterpenoids and 5-hydroxymethylfurfural and vanillin, respectively, and dauricanols D(5) and E(6) represent the first examples of 6-deoxy-1,5-seco-grayanane diterpenoids. Their structures were determined by spectroscopic methods, quantum chemical calculation including ^(13)C NMR-DP4+ analysis and ECD calculation, and single-crystal X-ray diffraction analysis. Plausible biosynthetic pathways for 1-4 were proposed. All the isolates showed significant analgesic activities,and dauricanols B(3) and C(4) showed more potent analgesic activities than the positive control, morphine.
基金This work was financially supported by the Scientific Research Project of Traditional Chinese Medicine of Hubei Provincial Health Commission(ZY2021M056)the Open Project of State Key Laboratory of Chemistry and Molecular Engineering of Medicinal Resources(No.CMEMR-2021-B03)。
文摘Kalmane diterpenoids,featuring a 5/8/5/5 tetracyclic carbon skeleton,are very rare in nature.The flowers of Rhododendron dauricum L.(Ericaceae)were phytochemically investigated for the first time,leading to the isolation of eight kalmane diterpenoids(1-8)including four new ones,named rhodokalmanols A-D(1-4).The structures of 1-8 were elucidated by comprehensive spectroscopic methods and ic NMR-DP4+analysis,and the absolute configurations of 1,2,4,and 5 were defined by single-crystal X-ray diffraction analysis with Cu Kαradiation.Rhodokalmanol A(1)represents the first 5,8-epoxykalmane diterpenoid and also the first kalm-15(16)-ene diterpenoid.Rhodokalmanols BD(2-4)are the first examples of kalm-7(8)-ene,kalm-16(17)-ene,and 8α-methoxykalmane diterpenoids,respectively.All the isolated kalmane diterpenoids 1-8 exhibited significant analgesic effects,and rhodokalmanol C(3)and kalmanoi(8)expressed more potent analgesic activity than morphine at doses of 0.2 and 0.04 mg/kg.The preliminary structure-activity relationships of kalmane diterpenoids as potent analgesics are discussed.
基金supported by the National Natural Science Foundation of China(No.81373956)
文摘The present study was designed to determine the major chemical constituents of the leaves of Rhododendron dauricum L. Compounds were isolated and purified by various chromatographic methods, and their structures were elucidated by physicochemical properties and spectral data. The present study identified two new C-methyl flavanones, 5, 7, 3', 5'-tetrahydroxy-6, 8-di-C-methyl flavanone(1) and 5, 4'-dihydroxy-8-C-methylflavanone-7-O-β-D-glucopyranoside(2), and one new flavonoid glycoside, quercetin-3-O-β-D-(6''-O-cinnamoyl)-galactoside(3), along with seven known compounds, including syzalterin(4), poriolin(5), farrerol-7-O-β-D-glucopyranoside(6), myrciacetin(7), quercetin-3-O-β-D-(6-p-hydroxy-benzoyl)-galactoside(8), quercetin-3-O-β-D-(6-p-coumaroyl)-galactoside(9), and 5, 7, 3', 5'-tetrahydroxyl flavanone(10). Compounds 1-3 were determined to be new flavonoids; compounds 4-6 were isolated from this species for the first time; and compounds 7-10 were reported for the first time from this genus.
